Hereditary Coproporphyria (HCP): Symptoms, Causes
Hereditary coproporphyria (HCP) is a rare genetic disorder characterized by a deficiency in the enzyme coproporphyrinogen oxidase (CPOX), which is crucial in the heme biosynthesis…
Acute Hepatic Porphyria: Symptoms, Causes, Diagnosis, and Treatment
Acute hepatic porphyria (AHP) is a group of rare genetic disorders characterized by the accumulation of porphyrins and their precursors in the liver, leading to…